Description

Prochlorperazine Edisylate is a high-purity pharmaceutical salt form of the potent phenothiazine derivative, prochlorperazine. This compound is a critical active pharmaceutical ingredient (API) valued for its antiemetic and antipsychotic properties. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of injectable and oral dosage forms for the treatment of severe nausea, vomiting, and certain psychiatric conditions.

Application

• Pharmaceutical API: Primary use as the active ingredient in the manufacture of finished dosage forms, particularly injectable solutions for rapid action.
• Antiemetic Formulations: Used in medications designed to control severe nausea and vomiting associated with chemotherapy, surgery, or other medical conditions.
• Antipsychotic Medications: Serves as a key component in formulations for managing symptoms of schizophrenia and other psychotic disorders.
• Research & Development: Employed in preclinical and clinical studies to investigate neurological pathways and develop new therapeutic agents.
• Reference Standard: Used in analytical laboratories as a high-purity standard for quality control testing of pharmaceutical products.
• Veterinary Pharmaceuticals: Applicable in the development of treatments for nausea and behavioral issues in animals.

Basic Information

Product Name	Prochlorperazine Edisylate
CAS No.	1257-78-9
Molecular Formula	C20H24ClN3S • C2H6O6S2
Molecular Weight	564.08 g/mol
Synonyms	Prochlorperazine Edisilate; Prochlorperazine Ethanedisulfonate; 2-Chloro-10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine Edisylate; Compazine Edisylate; Stemetil; Novamin; Chlorperazine Edisylate; Prochlorperazine Dimaleate (related salt)
EINECS	215-014-9

Quality Control

Our Prochlorperazine Edisylate is manufactured under strict quality management systems. Each batch is tested to ensure it meets stringent specifications for identity, purity, and potency, aligning with pharmacopeial standards such as USP and EP. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to standard
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.